A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6944631



Internal ID9706556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:110226355..110226744hg38UCSC Ensembl
Outerchr10:111986113..111986502hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740795
Supporting Variants
SamplesSSM023
Known GenesMXI1
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6944631
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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